FDA label 38b3b032-17d8-4ef7-989c-efd48948723d

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID: 0d38d86b-90a6-4e09-9980-4c322faa5c15
SPL ID: 38b3b032-17d8-4ef7-989c-efd48948723d
Version: 5
Effective date: 2013-05-22
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:33:36

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		38b3b032-17d8-4ef7-989c-efd48948723d	id
spl set id		0d38d86b-90a6-4e09-9980-4c322faa5c15	set_id

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings for external use only STOP USE AND ASK A DOCTOR IF condition wors ens symptoms persist for more than 7 days or clear up and occur again within a few days redness is present irritation develops IF PREGNANT OR BREAST-FEEDING ask a health professional before use. When using this product use only as directed do not bandage tightly or use with a heating pad avoid contact with eyes or mucous membranes do not apply to wounds or damaged skin Keep out of reach of children In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.